Canonical Allele Identifier: PA2828475791
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 414648
ClinVar RCV Id: RCV000459636 RCV001293002 RCV001821327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.His377Arg
CA2249505
NM_001374253.1:c.1130A>G